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rs863224265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTC;GTC) 0 common in clinvar
(TCG;TCG) 0 common in clinvar
Make rs863224265(-;-)
Make rs863224265(-;GTC)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301038
GeneWFS1
is asnp
is mentioned by
dbSNPrs863224265
ClinGenrs863224265
ebirs863224265
HLIrs863224265
Exacrs863224265
Varsomers863224265
Maprs863224265
PheGenIrs863224265
hapmaprs863224265
1000 genomesrs863224265
hgdprs863224265
ensemblrs863224265
gopubmedrs863224265
geneviewrs863224265
scholarrs863224265
googlers863224265
pharmgkbrs863224265
gwascentralrs863224265
openSNPrs863224265
23andMers863224265
23andMe allrs863224265
SNP Nexus

SNPshotrs863224265
SNPdbers863224265
MSV3drs863224265
GWAS Ctlgrs863224265
Max Magnitude0
ClinVar
Risk rs863224265(-;-) Rs863224265(TCG;TCG)
Alt rs863224265(-;-) Rs863224265(TCG;TCG)
Reference Rs863224265(GTC;GTC)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302765_6302767delGTC
CLNSRC
CLNACC RCV000199829.1,